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Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism
AIMS: Whether diabetes increases venous thromboembolism (VTE) is unclear. Any greater risk may relate to insulin resistance, but many studies did not differentiate between type 1 diabetes and type 2 diabetes for VTE risk. METHODS: Retrospective cohort study of the Royal College of General Practition...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247424/ https://www.ncbi.nlm.nih.gov/pubmed/33165941 http://dx.doi.org/10.1111/dme.14452 |
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author | Hinton, William Nemeth, Banne de Lusignan, Simon Field, Ben Feher, Michael D. Munro, Neil Roberts, Lara N. Arya, Roopen Whyte, Martin B. |
author_facet | Hinton, William Nemeth, Banne de Lusignan, Simon Field, Ben Feher, Michael D. Munro, Neil Roberts, Lara N. Arya, Roopen Whyte, Martin B. |
author_sort | Hinton, William |
collection | PubMed |
description | AIMS: Whether diabetes increases venous thromboembolism (VTE) is unclear. Any greater risk may relate to insulin resistance, but many studies did not differentiate between type 1 diabetes and type 2 diabetes for VTE risk. METHODS: Retrospective cohort study of the Royal College of General Practitioners Research and Surveillance Centre, comprising over 530 primary care practices. We determined whether type 1 diabetes and/or type 2 diabetes are independent risk factors for VTE. The index date was 1 January 2009, individuals were followed to 31 December 2018, or censoring. Cox proportional hazard regression analysis was used to investigate the risk of VTE in people with type 1 diabetes and type 2 diabetes relative to no diabetes. The primary outcome was occurrence of VTE. The model was adjusted for potential confounders for VTE. RESULTS: There were 7086 people with type 1 diabetes and 95,566 with type 2 diabetes, diagnosed before 1 January 2009. The non‐diabetes group consisted of 1,407,699 people. In the unadjusted analysis, there was no increased risk of VTE with type 1 diabetes (HR 1.00, 95% CI 0.76–1.33) but there was for type 2 diabetes (HR 2.70, 95% CI 2.57–2.84). In the fully adjusted model, VTE risk was increased in type 1 diabetes (HR 1.46, 95% CI 1.11–1.92), but not with type 2 diabetes (HR 1.06, 95% CI 0.98–1.14). CONCLUSIONS: Type 1 diabetes was associated with a greater risk for VTE while type 2 diabetes was not. Further work is needed to determine the reason(s) for this. |
format | Online Article Text |
id | pubmed-8247424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82474242021-07-02 Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism Hinton, William Nemeth, Banne de Lusignan, Simon Field, Ben Feher, Michael D. Munro, Neil Roberts, Lara N. Arya, Roopen Whyte, Martin B. Diabet Med Research: Complications AIMS: Whether diabetes increases venous thromboembolism (VTE) is unclear. Any greater risk may relate to insulin resistance, but many studies did not differentiate between type 1 diabetes and type 2 diabetes for VTE risk. METHODS: Retrospective cohort study of the Royal College of General Practitioners Research and Surveillance Centre, comprising over 530 primary care practices. We determined whether type 1 diabetes and/or type 2 diabetes are independent risk factors for VTE. The index date was 1 January 2009, individuals were followed to 31 December 2018, or censoring. Cox proportional hazard regression analysis was used to investigate the risk of VTE in people with type 1 diabetes and type 2 diabetes relative to no diabetes. The primary outcome was occurrence of VTE. The model was adjusted for potential confounders for VTE. RESULTS: There were 7086 people with type 1 diabetes and 95,566 with type 2 diabetes, diagnosed before 1 January 2009. The non‐diabetes group consisted of 1,407,699 people. In the unadjusted analysis, there was no increased risk of VTE with type 1 diabetes (HR 1.00, 95% CI 0.76–1.33) but there was for type 2 diabetes (HR 2.70, 95% CI 2.57–2.84). In the fully adjusted model, VTE risk was increased in type 1 diabetes (HR 1.46, 95% CI 1.11–1.92), but not with type 2 diabetes (HR 1.06, 95% CI 0.98–1.14). CONCLUSIONS: Type 1 diabetes was associated with a greater risk for VTE while type 2 diabetes was not. Further work is needed to determine the reason(s) for this. John Wiley and Sons Inc. 2020-11-27 2021-05 /pmc/articles/PMC8247424/ /pubmed/33165941 http://dx.doi.org/10.1111/dme.14452 Text en © 2020 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research: Complications Hinton, William Nemeth, Banne de Lusignan, Simon Field, Ben Feher, Michael D. Munro, Neil Roberts, Lara N. Arya, Roopen Whyte, Martin B. Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title | Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title_full | Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title_fullStr | Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title_full_unstemmed | Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title_short | Effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
title_sort | effect of type 1 diabetes and type 2 diabetes on the risk of venous thromboembolism |
topic | Research: Complications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247424/ https://www.ncbi.nlm.nih.gov/pubmed/33165941 http://dx.doi.org/10.1111/dme.14452 |
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